Specifi Cations - GCE Healthcare M50 Manual De Usuario

5. LCD, ALARM AND TROUBLESHOOTING GUIDE
Technical Specifi cations
Model
Rated power (W)
EN
Electrical requirements
Flow rate (l/min)
Purity
Outlet pressure
Dimensions
Net weight
Sound level
Expected service life
Equipment class and type
Features
Disposal
Dispose of this device in accordance with local regulations.
Standards compliance
This device is designed to conform to the following standards:
• IEC 60601-1 Medical Electrical Equipment - Part 1: General requirements for basic safety and essential
performance
• IEC 60601-1-2: 2014 2nd edition, Medical Electrical Equipment, Part 1-2: General Requirement for Safety -
Collateral Standard: Electromagnetic Compatibility - Requirements and Tests
• IEC 60601-1-8: 2012 Medical electrical equipment - Part 1-8: General requirements for basic safety and es-
sential performance - Collateral Standard: General requirements, tests and guidance for alarm systems in
medical electrical equipment and medical electrical systems +Amendment 1:2012
• IEC 60601-1-11: 2015 Medical electrical equipment - Part 1-11: General requirements for basic safety and
essential performance - Collateral Standard: Requirements for medical electrical equipment and medical
electrical systems used in the home healthcare environment
• BS EN ISO 80601-2-69: 2014 Medical electrical equipment - Part 2-69: Particular requirements for basic
safety and essential performance of oxygen concentrator equipment
M50
300 (1.5A)
310 (3A) (North America)
220V (+/- 10%) 50Hz (+/- 10%)
220V (+/- 10%) 60Hz (+/- 10%)
115V (+/- 10%) 60Hz (+/- 10%)
0.5 to 5
87% to 96%
0.05±10% MPa
390 mm x 230 mm x 600 mm
15.2 kg
42 dBA
5 years
IEC Class II Equipment
Type BF Applied Part
IP21 Drip Proof
Standard: Abnormal temperature alarm; low
oxygen concentration alarm; power failure alarm;
timer; no fl ow alarm
Additional: Positive pressure outlet
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